SNP Detail For rs6868223
1.Mapping Information
Human SNP ID rs6868223
Human chromosome chr5
Human SNP position 33636489
Pig chromosome chr16
Pig SNP position 20435851
2.Annotation Information
PubMed ID20400778
JournalCirc Cardiovasc Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/20400778
StudyGenomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.
Disease/TraitMortality in heart failure
Initial sample1,645 European ancestry cases, 881 European ancestry controls, 281 African ancestry cases, 185 African ancestry controls
Replication sampleNA
Region5p13.3
Chromosome idchr5
Chromosome position33636489
Reported geneADAMTS12
Mapped geneADAMTS12
Upstream gene id
Downstream gene id
SNP gene ids81792
Upstream gene distance
Downstream gene distance
SNP risk allelers6868223-A
SNPsrs6868223
Merged0
SNP id current6868223
Contextintron_variant
Intergenic0
Allele frequency0.338
P value0.000002
Pvalue mlog5.69897000433601
P value text(AA)
Or beta1.58
%95 Ci[0.98-2.56]
PlatformAffymetrix [up to 2366858] (imputed)
CNVN
Mapped traitheart failure, mortality
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003144, http://www.ebi.ac.uk/efo/EFO_0004352
Study accessionGCST000661